10 results
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34ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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REVERSO
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
De Soutter Medical
FDA UDI
DE SOUTTER MEDICAL LIMITED·05051471193444·K-WIRE - SINGLE TROCAR 3.0mm DIA x 150mm
DUPONT DRUG CALIBRATOR-A
FDA 510(k)
FDA Class 1
·Clinical Chemistry
LATEX EXAMINATION GLOVES
FDA 510(k)
FDA Class 1
·General Hospital
INFUSE BMP
FDA Adverse Event
Injury
·MEDTRONIC·Product code NEK·March 2, 2013
HERCULES 3 STAGE ESOPHAGEAL BALLOON
FDA Adverse Event
Malfunction
·WILSON-COOK MEDICAL, INC.·Product code KNQ·January 14, 2011
SENSIA DR
FDA Adverse Event
Injury
·IPG MFG SWITZERLAND·Product code NVZ·August 8, 2014
23GA ILLUMINATED DIRECTIONAL LASER PROBE
FDA Adverse Event
Injury
·BAUSCH + LOMB·Product code HQB·March 19, 2020
25GA ILLUMINATED DIRECTIONAL LASER PROBE
FDA Adverse Event
Injury
·BAUSCH + LOMB·Product code HQB·March 19, 2020
Accolade TMZF Plus Hip Stem: Catalog # 3020-0537 Accolate d TMZF Hip Stem # 5 Catalog #6020-3535 Accolade 132 Size 3.5 Catalog # 6021-0230 Accolade Plus TMZF Hip Stem #2 Catalog # 6021-0335 Accolade Plus TMZF Hip Stem #3 Catalog #3021-0435 Accolade TMZF Hip Stem #4 Catalog # 6021-0435 Accolade Plus TMZF Hip Stem #4 Catalog #6021-2530 Accolade (127 deg) Size 2.5 Accolade (127 deg) Size 2.5 Catalog # 6021-4535 Accolade (127 DEG) Size 4.5 K994366; k023105; K032300 Manufactured by " Stryker Ireland, Carrigtwohill Industrial Estate Carrington County Cork, Ireland The subject hip stem is a single-use device intended for the reconstruction of the head and neck of the femoral joint. This hip stem is intended for primary reconstruction of the proximal femur or revision total hip arthroplasty.
FDA Recall
Terminated
·Stryker Howmedica Osteonics Corp.·Product code ISL·March 1, 2011